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Zymo Research Corporation
Quick SARS-CoV-2 Multiplex Kit

Compatibility - Compatible with automated and high-throughput workflows
Equipment Required - Real-Time PCR Instruments capable of detecting HEX/VIC and Quasar® 670/Cy5 fluorophores. Adjustments of the RT-PCR parameters may be necessary for instruments different than the CFX96 Touch from Bio-Rad
Input Quality - Purified RNA free of enzymatic inhibitors
Processing Time - ≤ 2 hours from set up to results
Reagents - Complete and ready to use master mix
Registration Status - CE-IVD Marked
Sample Input Material - Purified RNA from upper respiratory and lower respiratory systems

High Sensitivity: Limit of Detection as low as 10 GEC/reaction (167 GEC/ml)

Rapid & Easy Setup: Ready-to-use Master Mix, just add sample.

Compatible with Automated and High-Throughput workflows.

CE-IVD Marked

The Quick SARS-CoV-2 Multiplex Kit is a real-time reverse transcription PCR (rRT-PCR) test for the qualitative detection of RNA from the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) which is responsible for the coronavirus disease (COVID-19).

The Quick SARS-CoV-2 rRT-PCR Kit targets a region of the viral nucleocapsid (N) gene and a host-specific target region (human RNase P gene) to assess sample quality. The kit also includes CV Positive Control that enable assay performance monitoring, and a No-Template Control to confirm the absence of contamination in the reagents.

The Quick SARS-CoV-2 Multiplex Kit can be used on purified RNA samples isolated from upper respiratory and lower respiratory systems.

The Quick SARS-CoV-2 Multiplex Kit has High Sensitivity, with a Limit of Detection as low as 10 viral genome equivalent copies per reaction, a fast turnaround time of less than 2 hours, and a simple workflow in which RNA is simply added to the Quick SARS-CoV-2 Multiplex Kit reagent and directly analyzed.

Due to its simplicity, set-up up can be performed in an automation and it is compatible with high-throughput platforms. The kit is compatible with multiple Real-Time PCR instruments capable of detecting HEX/VIC and Quasar 670/Cy5 fluorophores and technical support is available for all steps of the setup process and data interpretation.

Note: In the United States, this test has not been FDA cleared or approved and it is currently CE IVD marked.


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